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MGAT1 Antibody (C-term)

Catalog Number:OM213674
OM213674
Discount Price
OM213674-100ul
1~2 Week
100ul
OM213674-50ul
50ul
OM213674-20ul
20ul
1~2 Week
Product Profile
Product Name MGAT1 Antibody (C-term)
Antibody Type Primary Antibodies
Antigen Alias MGAT1; GGNT1; GLCT1; GLYT1; MGAT; Alpha-1, 3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase; N-glycosyl-oligosaccharide-glycoprotein N-acetylglucosaminyltransferase I
Key Feature
Clonality Polyclonal
Isotype Ig
Host Species Rabbit
Tested Applications WBIHC
WB:1:100~500 IHC
Species Reactivity Human
Concentration 1mg/ml
Target Information
Gene Synonyms GGNT1
GLCT1
GLYT1
MGAT
Alternative Names MGAT1
GGNT1
GLCT1
GLYT1
MGAT
Alpha-1
3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase
N-glycosyl-oligosaccharide-glycoprotein N-acetylglucosaminyltransferase I
Molecular Weight(MW) 50878 Da
Function Initiates complex N-linked carbohydrate formation. Essential for the conversion of high-mannose to hybrid and complex N-glycans
Tissue Specificity Appears to be present in all tissues.
Cellular Localization Golgi apparatus membrane; Single-pass type II membrane protein
Database Links
Entrez Gene 4245
Nucleotide Accession NP_002397
Application

Application

Western blot analysis of anti-hMGAT1-R426 Pab in Y79 cell line lysate. hMGAT1-R426(arrow) was detected using the purified Pab.

Application

Formalin-fixed and paraffin-embedded human cancer tissue reacted with the primary antibody, which was peroxidase-conjugated to the secondary antibody, followed by AEC staining. This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated. BC = breast carcinoma; HC = hepatocarcinoma.
Application Notes WB:1:100~500 IHC
Additional Information
Form Liquid
Storage Instructions For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
Storage Buffer Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein G column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS.
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